Kálmán B - Search Results

1

[Vanishing white matter disease, a rare leukodystrophy with mutation in the EIF2B5 gene].

Sinkó G, Tompa M, Kiss Z, Kálmán B. Sinkó G, et al. Among authors: kalman b. Ideggyogy Sz. 2024 May 30;77(5-6):207-211. doi: 10.18071/isz.77.0207. Ideggyogy Sz. 2024. PMID: 38829246 Free article. Hungarian.

2

Is the mitochondrial DNA involved in determining susceptibility to multiple sclerosis?

Kalman B, Alder H. Kalman B, et al. Acta Neurol Scand. 1998 Oct;98(4):232-7. doi: 10.1111/j.1600-0404.1998.tb07301.x. Acta Neurol Scand. 1998. PMID: 9808271 Review.

3

Genetic variants of Complex I in multiple sclerosis.

Vyshkina T, Banisor I, Shugart YY, Leist TP, Kalman B. Vyshkina T, et al. Among authors: kalman b. J Neurol Sci. 2005 Jan 15;228(1):55-64. doi: 10.1016/j.jns.2004.09.027. J Neurol Sci. 2005. PMID: 15607211

4

[Clinical value of two methods to measure parathyroid hormone in chronic renal insufficiency, considering vitamin D metabolism].

Kovács L, Virágh E, Balogh D, Kálmán B, Lőcsei Z, Toldy E. Kovács L, et al. Among authors: kalman b. Orv Hetil. 2013 Dec 22;154(51):2025-36. doi: 10.1556/OH.2013.29784. Orv Hetil. 2013. PMID: 24334134 Hungarian.

5

Two sisters with multiple sclerosis, lamellar ichthyosis, beta thalassaemia minor and a deficiency of factor VIII.

Capra R, Mattioli F, Kalman B, Marcianò N, Berenzi A, Benetti A. Capra R, et al. Among authors: kalman b. J Neurol. 1993 Jun;240(6):336-8. doi: 10.1007/BF00839963. J Neurol. 1993. PMID: 8336172

6

Sclerosis multiplex in gypsies.

Kálmán B, Takács K, Gyódi E, Kramer J, Füst G, Tauszik T, Guseo A, Kuntár L, Komoly S, Nagy C, et al. Kálmán B, et al. Acta Neurol Scand. 1991 Sep;84(3):181-5. doi: 10.1111/j.1600-0404.1991.tb04934.x. Acta Neurol Scand. 1991. PMID: 1683089

7

Characteristics of the T lymphocytes involved in experimental allergic encephalomyelitis.

Kalman B, Alder H, Lublin FD. Kalman B, et al. J Neuroimmunol. 1995 Sep;61(2):107-16. doi: 10.1016/0165-5728(95)00109-f. J Neuroimmunol. 1995. PMID: 7593546 Review.

8

Striking pathology in Leigh syndrome associated with the MTATP6 T8993G mutation.

Sinko G, Garzuly F, Kalman B. Sinko G, et al. Among authors: kalman b. Pediatr Neurol. 2014 Oct;51(4):585-6. doi: 10.1016/j.pediatrneurol.2014.07.015. Epub 2014 Jul 19. Pediatr Neurol. 2014. PMID: 25152966 No abstract available.

9

[Nusinersen in the treatment of spinal muscular atrophy].

Sinkó G , Kiss Z , Kalman B . Sinkó G , et al. Among authors: kalman b. Ideggyogy Sz. 2018 Mar 30;71(3-04):90-94. doi: 10.18071/isz.71.0090. Ideggyogy Sz. 2018. PMID: 29889467 Free article. Review. Hungarian.

10

Isocitrate dehydrogenase mutations in defining the biology of and supporting clinical decision making in glioblastoma.

Kálovits F , Tompa M , Nagy Á , Kálmán B . Kálovits F , et al. Among authors: kalman b. Ideggyogy Sz. 2018 Jul 30;71(7-08):237-247. doi: 10.18071/isz.71.0237. Ideggyogy Sz. 2018. PMID: 30113792 Free article. Review. English.

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